Clinical Trials Directory

Trials / Completed

CompletedNCT02507700

Popliteal Block for Postoperative Pain in Knee-ankle Soft Tissue Surgery in Cerebral Palsy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Diskapi Teaching and Research Hospital · Academic / Other
Sex
All
Age
3 Years – 15 Years
Healthy volunteers
Not accepted

Summary

Popliteal block is a technique for providing postoperative pain management in children. In this randomized double-blinded study, the investigators evaluated the effects of preoperative popliteal nerve block on postoperative pain and analgesic requirement in children with cerebral palsy (CP) undergoing knee-anckle soft tissue surgery. The Wong Baker faces scale and skin conductance fluctuations will be assessed.

Detailed description

Sevoflurane will be used for anesthesia induction and maintance. Laryngeal mask airway will be placed without neuromuscular blocking agent. In group P (popliteal block), a single dose of 0.3ml.kg(-1) of 0.25% bupivacaine will be performed for popiteal nerve block (with ultrasound guidence). In group C ( control), only plaster cover will be applied without nerve block for sham procedure to provide double-blinded study. Intraoperative heart rate, mean arterial pressure, BIS (bispectral index) values, sevoflurane consumption will be recorded ten minutes interval. Wong Baker faces scale and skin conductance fluctuations will be recorded at postoperative 0, 10th min, 20th min , 1st h, 4th h, 12th h qnd 24th h. Total analgesic consumption (paracetamol orally ) will be recorded.

Conditions

Interventions

TypeNameDescription
PROCEDUREPopliteal blockIn group P, popliteal block will be performed with ultrasound guidence.
DRUGSevofluraneSevoflurane will be used to all patient's for anesthesia induction and maintenance
DEVICEUltrasoundFor recognize the nerve (sciatic nerve), ultrasound will be used in group P.
OTHERPlaster coverPlaster cover will be used to control group for sham procedure
DRUGbupivacaineBupivacaine 0.25% will be performed for popliteal block to group P.
OTHERLaryngeal mask airwayAfter anesthesia induction, laryngeal mask airway will be inserted to all patients

Timeline

Start date
2015-06-01
Primary completion
2016-05-01
Completion
2016-06-01
First posted
2015-07-24
Last updated
2016-06-13

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT02507700. Inclusion in this directory is not an endorsement.